Abdominal Angiography

2016 ◽  
pp. 820-841
Author(s):  
Kyung Jae Cho
1988 ◽  
Vol 100 (11-12) ◽  
pp. 1137-1140
Author(s):  
Ichiroh HINO ◽  
Motoomi OHKAWA ◽  
Kanji KOJIMA ◽  
Hiroyuki SEO ◽  
Katashi SATOH ◽  
...  

2009 ◽  
Vol 75 (4) ◽  
pp. 331-334 ◽  
Author(s):  
Yoshitaka Toyomasu ◽  
Minoru Fukuchi ◽  
Takatomo Yoshida ◽  
Kohei Tajima ◽  
Hidenobu Osawa ◽  
...  

An 82-year-old man was admitted to our hospital with a complaint of hypoglycemic syncope in the early morning. Insulinoma was suspected, but an abdominal CT showed no mass. Abdominal angiography showed a slight stain fed from the splenic artery. Arterial stimulation and venous sampling (ASVS) showed an abnormal insulin response only from the splenic artery. Under a provisional diagnosis of insulinoma, surgical treatment was undertaken. Although no pancreatic masses were palpable, we performed a distal pancreatectomy. Subsequently, a pathological examination revealed diffuse nesidioblastosis. Reported cases of diffuse nesidioblastosis have had common clinical features: postprandial hyperinsulinemic hypoglycemia, no abnormal findings in radiological examinations, and the presence of the ductulo-insular complex on histological examination. Surgical resection is recommended, but the extent of surgery is controversial. Our case had some clinical features of insulinoma but was diagnosed as diffuse nesidioblastosis according to histopathologic criteria. Because ASVS showed that the pancreatic body and tail had a lesion producing insulin abnormally, we performed a distal pancreatectomy to cure the hypoglycemia. Clinically, it is very difficult to distinguish diffuse nesidioblastosis from insulinoma. When we treat hyperinsulinemic hypoglycemia, ASVS can be an essential examination to decide the extent of pancreatectomy.


Gut ◽  
1965 ◽  
Vol 6 (5) ◽  
pp. 477-486 ◽  
Author(s):  
M J Laurijssens ◽  
J T Galambos

2019 ◽  
pp. 195-222
Author(s):  
Gratian Dragoslav Miclaus ◽  
Horia Ples

2019 ◽  
Vol 12 (7) ◽  
pp. e229491
Author(s):  
Shinichiro Sakaki ◽  
Taiyu Hayashi ◽  
Hiroshi Ono

A 5-month-old girl with single ventricle, interrupted inferior vena cava and polysplenia syndrome palliated with bilateral Blalock-Taussig shunts developed severe cyanosis despite apparently increased pulmonary blood flow. Angiography revealed diffuse pulmonary arteriolar capillary dilatation and early pulmonary venous filling, suggesting the presence of pulmonary arteriovenous malformations. Abdominal angiography at 6 months demonstrated a large extrahepatic portosystemic shunt, which was percutaneously closed with a vascular plug. Kawashima operation was performed 2 weeks after portosystemic shunt closure. Although cyanosis improved temporarily, the patient suffered from deteriorating cyanosis at 9 months of age and underwent Fontan completion. Thereafter, her oxygen saturation gradually improved to 95% over the course of 3 weeks. Both the congenital extrahepatic portosystemic shunt and Kawashima operation contributed to the development of pulmonary arteriovenous malformations.


Radiology ◽  
1979 ◽  
Vol 131 (1) ◽  
pp. 251-251 ◽  
Author(s):  
Jonathan M. Levy ◽  
Patrick F. Sheedy ◽  
Richard E. Fulton ◽  
Anthony W. Stanson

1977 ◽  
Vol 18 (1) ◽  
pp. 55-64 ◽  
Author(s):  
K. Jonsson ◽  
A. Lunderquist ◽  
H. Pettersson ◽  
B. Sigstedt

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